GlyCosmos Portal

Danio rerio (zebrafish)

Summary

Taxonomy ID: 7955
PubChem Taxonomy: 7955

Genes (358) Glycans (175) Glycoproteins (592) Lectins (18) Pathways (252)

Displaying entries **226 - 250** of **358** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
678597	UDP glucuronosyltransferase 5 family, polypeptide B6	ugt5b6
724006	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	mgat5	proteinuria
724080	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 5	b4galt5	multiple sclerosis
751635	ALG5 dolichyl-phosphate beta-glucosyltransferase	alg5	polycystic kidney disease
751653	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 4	st6galnac4
751669	UDP glucuronosyltransferase 5 family, polypeptide C2	ugt5c2
767705	UDP glucuronosyltransferase 2 family, polypeptide A5	ugt2a5
767756	UDP glucuronosyltransferase 5 family, polypeptide A2	ugt5a2
768121	forkhead box O1 a	foxo1a	Parkinson's disease alveolar rhabdomyosarcoma congestive heart failure hepatocellular carcinoma metabolic dysfunction-associated steatotic liver disease prostate cancer
768123	DP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1, like	b4galt1l	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease
777616	zgc:154054	zgc:154054
777617	protein-glucosylgalactosylhydroxylysine glucosidase	pgghg
777668	protein O-fucosyltransferase 2	pofut2	Down syndrome
790919	glucose-6-phosphatase catalytic subunit 3	g6pc3	severe congenital neutropenia 4
791107	heparan sulfate 6-O-sulfotransferase 1b	hs6st1b	hypogonadotropic hypogonadism 15 with or without anosmia
791188	heparan sulfate 2-O-sulfotransferase 1a	hs2st1a
791210	UDP glucuronosyltransferase 5 family, polypeptide B4	ugt5b4
791470	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5b	b3gnt5b
791613	UDP glucuronosyltransferase 2 family, polypeptide A4	ugt2a4
791759	phosphatidylinositol glycan anchor biosynthesis, class A	piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
792063	alpha(1,3)fucosyltransferase gene 2	ft2	candidiasis
792506	UDP glucuronosyltransferase 2 family, polypeptide B6	ugt2b6
792524	heparan sulfate 6-O-sulfotransferase 3a	hs6st3a
792692	aldolase C, fructose-bisphosphate, a	aldoca	autoimmune disease of the nervous system borna disease hepatocellular carcinoma
793362	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2b	b3gnt2b

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